Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Jeppe Falsig"'
Autor:
Uli S Herrmann, Tiziana Sonati, Jeppe Falsig, Regina R Reimann, Paolo Dametto, Tracy O'Connor
Publikováno v:
PLoS Pathogens, Vol 11, Iss 4, p e1004808 (2015)
[This corrects the article DOI: 10.1371/journal.ppat.1004662.].
Externí odkaz:
https://doaj.org/article/cad35e58d6524f12b325279b629c74d4
Autor:
Uli S Herrmann, Tiziana Sonati, Jeppe Falsig, Regina R Reimann, Paolo Dametto, Tracy O'Connor, Bei Li, Agnes Lau, Simone Hornemann, Silvia Sorce, Uli Wagner, Despina Sanoudou, Adriano Aguzzi
Publikováno v:
PLoS Pathogens, Vol 11, Iss 2, p e1004662 (2015)
Prions induce lethal neurodegeneration and consist of PrPSc, an aggregated conformer of the cellular prion protein PrPC. Antibody-derived ligands to the globular domain of PrPC (collectively termed GDL) are also neurotoxic. Here we show that GDL and
Externí odkaz:
https://doaj.org/article/2f192076206246ed93ed98f65be2e327
Autor:
Silvia Sorce, Mario Nuvolone, Annika Keller, Jeppe Falsig, Ahmet Varol, Petra Schwarz, Monika Bieri, Herbert Budka, Adriano Aguzzi
Publikováno v:
PLoS Pathogens, Vol 10, Iss 12, p e1004531 (2014)
Prion infections cause neurodegeneration, which often goes along with oxidative stress. However, the cellular source of reactive oxygen species (ROS) and their pathogenetic significance are unclear. Here we analyzed the contribution of NOX2, a promin
Externí odkaz:
https://doaj.org/article/f7bf2f11417b42cb9f57bed8d329e3b5
Autor:
Jeppe Falsig, Tiziana Sonati, Uli S Herrmann, Dino Saban, Bei Li, Karina Arroyo, Boris Ballmer, Pawel P Liberski, Adriano Aguzzi
Publikováno v:
PLoS Pathogens, Vol 8, Iss 11, p e1002985 (2012)
Prions cause neurodegeneration in vivo, yet prion-infected cultured cells do not show cytotoxicity. This has hampered mechanistic studies of prion-induced neurodegeneration. Here we report that prion-infected cultured organotypic cerebellar slices (C
Externí odkaz:
https://doaj.org/article/4d93c9906020487fbbfde99e7148a661
Autor:
Lone Helboe, Nina Rosenqvist, Christiane Volbracht, Lars Ø. Pedersen, Jan T. Pedersen, Søren Christensen, Jan Egebjerg, Claus T. Christoffersen, Benny Bang-Andersen, Thomas G. Beach, Geidy E. Serrano, Jeppe Falsig
Publikováno v:
Journal of Alzheimer's Disease. 88:207-228
Background: Deposits of hyperphosphorylated tau fibrils are hallmarks of a broad spectrum of tauopathies, including Alzheimer’s disease (AD). Objective: To investigate heterogeneity of tau pathology across brain extracts from a broad selection of d
Autor:
Karsten Skjødt, Jan Egebjerg, Jan Torleif Pedersen, Fredrik Kartberg, Christiane Volbracht, Florence Sotty, Nina Helen Rosenqvist, Lars Østergaard Pedersen, Einar M. Sigurdsson, Ayodeji A. Asuni, Pia Jul, Christian Rungsted Andersson, Jeppe Falsig, Lone Helboe, Jeffrey B. Stavenhagen, Justus Claus Alfred Daechsel, Søren Christensen
Publikováno v:
Alzheimer's & Dementia : Translational Research & Clinical Interventions
Rosenqvist, N, Asuni, A A, Andersson, C R, Christensen, S, Daechsel, J A, Egebjerg, J, Falsig, J, Helboe, L, Jul, P, Kartberg, F, Pedersen, L Ø, Sigurdsson, E M, Sotty, F, Skjødt, K, Stavenhagen, J B, Volbracht, C & Pedersen, J T 2018, ' Highly specific and selective anti-pS396-tau antibody C10.2 targets seeding-competent tau ', Alzheimer's & Dementia: Translational Research & Clinical Interventions, vol. 4, pp. 521-534 . https://doi.org/10.1016/j.trci.2018.09.005
Rosenqvist, N, Asuni, A A, Andersson, C R, Christensen, S, Daechsel, J A, Egebjerg, J, Falsig, J, Helboe, L, Jul, P, Kartberg, F, Pedersen, L Ø, Sigurdsson, E M, Sotty, F, Skjødt, K, Stavenhagen, J B, Volbracht, C & Pedersen, J T 2018, ' Highly specific and selective anti-pS396-tau antibody C10.2 targets seeding-competent tau ', Alzheimer's & Dementia: Translational Research & Clinical Interventions, vol. 4, pp. 521-534 . https://doi.org/10.1016/j.trci.2018.09.005
Introduction: The abnormal hyperphosphorylation of the microtubule-associated protein tau plays a crucial role in neurodegeneration in Alzheimer's disease (AD) and other tauopathies.Methods: Highly specific and selective anti-pS396-tau antibodies hav
Autor:
Jeppe Falsig, Adriano Aguzzi
Publikováno v:
Nature Neuroscience
Prion science has been on a rollercoaster for two decades. In the mid 1990s, the specter of mad cow disease (bovine spongiform encephalopathy, BSE) provoked an unprecedented public scare that was first precipitated by the realization that this animal
Autor:
Mario Nuvolone, Adriano Aguzzi, Osvaldo Mirante, Isabelle M. Mansuy, Rita Moos, Mélissa Farinelli, Jeppe Falsig, Anna Maria Calella
Publikováno v:
EMBO Molecular Medicine
Alzheimer's disease (AD), the most common neurodegenerative disorder, goes along with extracellular amyloid-beta (Abeta) deposits. The cognitive decline observed during AD progression correlates with damaged spines, dendrites and synapses in hippocam
Publikováno v:
HFSP Journal. 2:332-341
Transmissible spongiform encephalopathies (TSEs) are lethal infectious neurodegenerative diseases. TSEs are caused by prions, infectious agents lacking informational nucleic acids, and possibly identical with higher-order aggregates of the cellular g
Autor:
Adriano Aguzzi, Jeppe Falsig
Publikováno v:
Nature Protocols. 3:555-562
Methods enabling prion replication ex vivo are important for advancing prion science. However, few such technologies exist and many prion strains are intractable with them. Here, we describe a prion organotypic slice culture assay (POSCA), which allo